ES2219812T3 - Productos salificados poliaminas y su empleo como dispersantes para pigmentos y cargas. - Google Patents

Productos salificados poliaminas y su empleo como dispersantes para pigmentos y cargas.

Info

Publication number: ES2219812T3
Authority: ES; Spain
Prior art keywords: polyamines; acid; mol; products; molecular weight
Prior art date: 1997-07-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

ES98113475T

Other languages

English (en)

Spanish (es)

Inventor

Karlheinz Haubennestel

Ulrich Dr. Orth

Wolfgang Dr. Pritschins

Udo Dr. Krappe

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BYK Chemie GmbH

Original Assignee

BYK Chemie GmbH

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1997-07-26

Filing date

1998-07-20

Publication date

2004-12-01

1998-07-20 Application filed by BYK Chemie GmbH filed Critical BYK Chemie GmbH

2004-12-01 Application granted granted Critical

2004-12-01 Publication of ES2219812T3 publication Critical patent/ES2219812T3/es

2018-07-20 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

229920000768 polyamine Polymers 0.000 title claims abstract description 108
239000002270 dispersing agent Substances 0.000 title claims abstract description 66
239000000049 pigment Substances 0.000 title claims abstract description 57
239000002253 acid Substances 0.000 claims abstract description 49
239000000203 mixture Substances 0.000 claims abstract description 41
150000001875 compounds Chemical class 0.000 claims abstract description 40
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical group CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 13
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
238000000034 method Methods 0.000 claims abstract description 8
230000004048 modification Effects 0.000 claims abstract description 8
238000012986 modification Methods 0.000 claims abstract description 8
150000003460 sulfonic acids Chemical class 0.000 claims abstract description 6
239000000047 product Substances 0.000 claims description 59
238000006243 chemical reaction Methods 0.000 claims description 37
125000001931 aliphatic group Chemical group 0.000 claims description 31
239000002966 varnish Substances 0.000 claims description 30
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 27
239000011230 binding agent Substances 0.000 claims description 26
125000003277 amino group Chemical group 0.000 claims description 22
239000012265 solid product Substances 0.000 claims description 22
150000002148 esters Chemical class 0.000 claims description 21
150000003014 phosphoric acid esters Chemical class 0.000 claims description 18
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 16
239000002245 particle Substances 0.000 claims description 16
239000000945 filler Substances 0.000 claims description 15
229920000642 polymer Polymers 0.000 claims description 14
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 12
125000003710 aryl alkyl group Chemical group 0.000 claims description 12
150000001412 amines Chemical class 0.000 claims description 11
125000003118 aryl group Chemical group 0.000 claims description 11
238000000576 coating method Methods 0.000 claims description 11
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims description 9
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239000000758 substrate Substances 0.000 claims description 9
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 8
229920001228 polyisocyanate Polymers 0.000 claims description 8
239000005056 polyisocyanate Substances 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
239000011248 coating agent Substances 0.000 claims description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
150000005676 cyclic carbonates Chemical class 0.000 claims description 6
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 6
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229920001519 homopolymer Polymers 0.000 claims description 5
239000012948 isocyanate Substances 0.000 claims description 5
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238000006116 polymerization reaction Methods 0.000 claims description 5
229910052757 nitrogen Inorganic materials 0.000 claims description 4
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150000001298 alcohols Chemical class 0.000 claims description 3
125000004185 ester group Chemical group 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
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125000001302 tertiary amino group Chemical group 0.000 claims description 3
125000002843 carboxylic acid group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 claims description 2
AQGNVWRYTKPRMR-UHFFFAOYSA-N n'-[2-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCNCCN AQGNVWRYTKPRMR-UHFFFAOYSA-N 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 2
238000006957 Michael reaction Methods 0.000 claims 1
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150000002170 ethers Chemical class 0.000 claims 1
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XPRXJFAFJFZWTC-UHFFFAOYSA-N hoso2 Chemical compound [O]S(O)=O XPRXJFAFJFZWTC-UHFFFAOYSA-N 0.000 claims 1
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
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150000007513 acids Chemical class 0.000 description 7
229920000728 polyester Polymers 0.000 description 6
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238000003756 stirring Methods 0.000 description 6
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ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 5
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239000003677 Sheet moulding compound Substances 0.000 description 5
150000001733 carboxylic acid esters Chemical class 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000007788 liquid Substances 0.000 description 5
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
229920000137 polyphosphoric acid Polymers 0.000 description 5
239000004071 soot Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
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150000005690 diesters Chemical class 0.000 description 4
238000005189 flocculation Methods 0.000 description 4
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238000005259 measurement Methods 0.000 description 4
239000012860 organic pigment Substances 0.000 description 4
235000015927 pasta Nutrition 0.000 description 4
229920000570 polyether Polymers 0.000 description 4
230000009467 reduction Effects 0.000 description 4
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
229920002873 Polyethylenimine Polymers 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000005054 agglomeration Methods 0.000 description 3
230000002776 aggregation Effects 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000835 fiber Substances 0.000 description 3
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 3
239000000463 material Substances 0.000 description 3
238000006366 phosphorylation reaction Methods 0.000 description 3
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239000000057 synthetic resin Substances 0.000 description 3
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QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-UHFFFAOYSA-N 0.000 description 2
238000005160 1H NMR spectroscopy Methods 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
239000000020 Nitrocellulose Substances 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
150000001541 aziridines Chemical class 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
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WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
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230000008034 disappearance Effects 0.000 description 1
238000004821 distillation Methods 0.000 description 1
PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000004519 grease Substances 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
235000012907 honey Nutrition 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000003999 initiator Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
238000011068 loading method Methods 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
239000000178 monomer Substances 0.000 description 1
RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
235000014594 pastries Nutrition 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
125000002270 phosphoric acid ester group Chemical group 0.000 description 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
230000000865 phosphorylative effect Effects 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000011164 primary particle Substances 0.000 description 1
230000000750 progressive effect Effects 0.000 description 1
YBTLJLASGKDJSG-UHFFFAOYSA-N prop-2-enoyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC(=O)C=C YBTLJLASGKDJSG-UHFFFAOYSA-N 0.000 description 1
229960000380 propiolactone Drugs 0.000 description 1
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
235000013570 smoothie Nutrition 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C08G73/0226—Quaternisation of polyalkylene(poly)amines
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/14—Derivatives of phosphoric acid
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/16—Amines or polyamines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Paints Or Removers (AREA)

ES98113475T 1997-07-26 1998-07-20 Productos salificados poliaminas y su empleo como dispersantes para pigmentos y cargas. Expired - Lifetime ES2219812T3 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19732251		1997-07-26
DE19732251A DE19732251B4 (de)	1997-07-26	1997-07-26	Versalzungsprodukte von Polyaminen und deren Einsatz als Dispergiermittel für Pigmente und Füllstoffe

Publications (1)

Publication Number	Publication Date
ES2219812T3 true ES2219812T3 (es)	2004-12-01

Family

ID=7837010

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES98113475T Expired - Lifetime ES2219812T3 (es)	1997-07-26	1998-07-20	Productos salificados poliaminas y su empleo como dispersantes para pigmentos y cargas.

Country Status (8)

Country	Link
US (1)	US6111054A (de)
EP (1)	EP0893155B1 (de)
JP (1)	JP4642166B2 (de)
AT (1)	ATE265267T1 (de)
CA (1)	CA2241773C (de)
DE (2)	DE19732251B4 (de)
DK (1)	DK0893155T3 (de)
ES (1)	ES2219812T3 (de)

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JP2785849B2 (ja) *	1990-03-29	1998-08-13	大倉工業株式会社	セメント成形板の製造方法
US6194539B1 (en) *	1994-11-22	2001-02-27	Daicel Chemical Industries, Inc.	Polylactone having amino groups, a process for the preparation thereof, a compound having amino group, a composition for coatings, a composition for printing inks

1997
- 1997-07-26 DE DE19732251A patent/DE19732251B4/de not_active Expired - Fee Related
1998
- 1998-06-26 US US09/105,975 patent/US6111054A/en not_active Expired - Lifetime
- 1998-06-29 CA CA002241773A patent/CA2241773C/en not_active Expired - Lifetime
- 1998-07-20 ES ES98113475T patent/ES2219812T3/es not_active Expired - Lifetime
- 1998-07-20 EP EP98113475A patent/EP0893155B1/de not_active Expired - Lifetime
- 1998-07-20 AT AT98113475T patent/ATE265267T1/de not_active IP Right Cessation
- 1998-07-20 DE DE59811262T patent/DE59811262D1/de not_active Expired - Lifetime
- 1998-07-20 DK DK98113475T patent/DK0893155T3/da active
- 1998-07-27 JP JP21071298A patent/JP4642166B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DE19732251A1 (de)	1999-01-28
DE19732251B4 (de)	2004-07-29
EP0893155A3 (de)	1999-05-26
JPH11114399A (ja)	1999-04-27
DE59811262D1 (de)	2004-06-03
EP0893155B1 (de)	2004-04-28
EP0893155A2 (de)	1999-01-27
CA2241773A1 (en)	1999-01-26
DK0893155T3 (da)	2004-07-26
JP4642166B2 (ja)	2011-03-02
CA2241773C (en)	2008-04-08
US6111054A (en)	2000-08-29
ATE265267T1 (de)	2004-05-15

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